A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050141



Internal ID21959374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37297169..37311711hg38UCSC Ensembl
chr19:37788071..37802613hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3814543
hg1914543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050141
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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